Curvafix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curvafix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CurvaFix Low Profile System, CurvaFix IM System, CurvaFix Intramedullary Rodscrew System
3
Total
3
Cleared
0
Denied
Curvafix, Inc. has 3 FDA 510(k) cleared medical devices. Based in Bellevue, US.
Latest FDA clearance: Aug 2025. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Curvafix, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by DuVal & Associates, P.A. and Backroads Consulting.
FDA 510(k) Regulatory Record - Curvafix, Inc.
3 devices